MICRO-NX Co., Ltd.

① Conduct regulatory management activities pertaining to the Company's medical devices ② Verify the compliance of manufactured devices in accordance with the quality management system before release ③ Maintain technical documents (Technical Document, TD) and EU Declaration of Conformity ④ Fulfill the obligations for post-market surveillance under the regulations of MDR(EU)2017/745 ⑤ Fulfill the reporting obligations in accordance with the Vigilance System Procedure

① Conduct regulatory management activities pertaining to the Company's medical devices ② Verify the compliance of manufactured devices in accordance with the quality management system before release ③ Maintain technical documents (Technical Document, TD) and EU Declaration of Conformity ④ Fulfill the obligations for post-market surveillance under the regulations of MDR(EU)2017/745 ⑤ Fulfill the reporting obligations in accordance with the Vigilance System Procedure